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Safety Analyses of the Phase 3 VISION Trial of [177Lu]Lu-PSMA-617 in Patients with Metastatic Castration-resistant Prostate Cancer.
Chi, Kim N; Armstrong, Andrew J; Krause, Bernd J; Herrmann, Ken; Rahbar, Kambiz; de Bono, Johann S; Adra, Nabil; Garje, Rohan; Michalski, Jeff M; Kempel, Mette M; Fizazi, Karim; Morris, Michael J; Sartor, Oliver; Brackman, Marcia; DeSilvio, Michelle; Wilke, Celine; Holder, Geoffrey; Tagawa, Scott T.
Afiliação
  • Chi KN; British Columbia Cancer, Vancouver Prostate Centre, Vancouver, Canada. Electronic address: kchi@bccancer.bc.ca.
  • Armstrong AJ; Duke Cancer Institute Center for Prostate & Urologic Cancers, Duke University, Durham, NC, USA.
  • Krause BJ; Department of Nuclear Medicine, Rostock University Medical Center, Rostock, Germany.
  • Herrmann K; Department of Nuclear Medicine, University of Duisburg-Essen, Essen, Germany; German Cancer Consortium (DKTK), University Hospital Essen, Essen, Germany.
  • Rahbar K; Department of Nuclear Medicine, University Hospital Münster, Münster, Germany.
  • de Bono JS; Division of Clinical Studies, The Institute of Cancer Research and The Royal Marsden Hospital, London, UK.
  • Adra N; Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN, USA.
  • Garje R; Miami Cancer Institute, Baptist Health South Florida, Miami, FL, USA.
  • Michalski JM; Department of Radiation Oncology, Washington University, St. Louis, MO, USA.
  • Kempel MM; Department of Oncology and Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
  • Fizazi K; Department of Cancer Medicine, Institut Gustave Roussy, University of Paris-Saclay, Villejuif, France.
  • Morris MJ; Genitourinary Oncology Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Sartor O; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, LA, USA.
  • Brackman M; Novartis Pharmaceuticals Corporation, Indianapolis, IN, USA.
  • DeSilvio M; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Wilke C; Novartis Pharma AG, Basel, Switzerland.
  • Holder G; Novartis Pharma AG, Basel, Switzerland.
  • Tagawa ST; Hematology and Medical Oncology Department, Weill Cornell Medicine, New York, NY, USA.
Eur Urol ; 85(4): 382-391, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38185538
ABSTRACT
BACKGROUND AND

OBJECTIVE:

[177Lu]Lu-PSMA-617 (177Lu-PSMA-617) plus the standard of care (SoC) significantly improved overall survival and radiographic progression-free survival versus SoC alone in patients with prostate-specific membrane antigen (PSMA)-positive metastatic castration-resistant prostate cancer in the VISION trial. We evaluated the safety of additional cycles of 177Lu-PSMA-617 and the impact of longer observation time for patients receiving 177Lu-PSMA-617 plus SoC.

METHODS:

VISION was an international, open-label study. Patients were randomised 21 to receive 177Lu-PSMA-617 plus SoC or SoC alone. The incidence of treatment-emergent adverse events (TEAEs) was assessed in prespecified subgroups of patients who received ≤4 cycles versus 5-6 cycles of treatment and during each cycle of treatment. The TEAE incidence was also adjusted for treatment exposure to calculate the incidence per 100 patient-treatment years of observation. This analysis was performed for the first occurrence of TEAEs. KEY FINDINGS AND

LIMITATIONS:

The any-grade TEAE incidence was similar in cycles 1-4 and cycles 5-6. TEAE frequency was similar across all cycles of 177Lu-PSMA-617 treatment. No additional safety concerns were reported for patients who received >4 cycles. The exposure-adjusted safety analysis revealed that the overall TEAE incidence was similar between arms, but distinct trends for different TEAE types were noted and the incidence of events associated with 177Lu-PSMA-617 remained higher in the 177Lu-PSMA-617 arm. CONCLUSIONS AND CLINICAL IMPLICATIONS Longer exposure to 177Lu-PSMA-617 plus SoC was not associated with a higher toxicity risk, and the extended time for safety observation could account for the higher TEAE incidence in comparison to SoC alone. The findings support a favourable benefit-risk profile for 6 cycles of 177Lu-PSMA-617 in this setting and the use of up to 6 cycles of 177Lu-PSMA-617 in patients who are clinically benefiting from and tolerating this therapy. PATIENT

SUMMARY:

For patients with metastatic prostate cancer no longer responding to hormone therapy, an increase in the number of cycles of treatment with a radioactive compound called 177Lu-PSMA-617 from four to six had no additional adverse side effects.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dipeptídeos / Neoplasias de Próstata Resistentes à Castração / Compostos Heterocíclicos com 1 Anel Tipo de estudo: Clinical_trials Limite: Humans / Male Idioma: En Revista: Eur Urol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dipeptídeos / Neoplasias de Próstata Resistentes à Castração / Compostos Heterocíclicos com 1 Anel Tipo de estudo: Clinical_trials Limite: Humans / Male Idioma: En Revista: Eur Urol Ano de publicação: 2024 Tipo de documento: Article